JSA REPROCESSED COMPRESSION SLEEVE DEVICES
K-Number: K031722 · 2003-11-25
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Device Summary
Frequently Asked Questions
What is the JSA REPROCESSED COMPRESSION SLEEVE DEVICES?
JSA REPROCESSED COMPRESSION SLEEVE DEVICES is a medical device that received FDA 510(k) clearance on 2003-11-25. The listed applicant is Jack Speer and Assoc., Inc.. The 510(k) number is K031722.
When did JSA REPROCESSED COMPRESSION SLEEVE DEVICES receive FDA 510(k) clearance?
JSA REPROCESSED COMPRESSION SLEEVE DEVICES received FDA 510(k) clearance on 2003-11-25, under 510(k) number K031722.
Who is the listed applicant for JSA REPROCESSED COMPRESSION SLEEVE DEVICES?
The FDA 510(k) record lists Jack Speer and Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JSA REPROCESSED COMPRESSION SLEEVE DEVICES?
The FDA product code for JSA REPROCESSED COMPRESSION SLEEVE DEVICES is JOW.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Jack Speer and Assoc., Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JOW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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